Canonical Allele Identifier: CA891839809
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957951_87957953delinsTTT , CM000672.2:g.87957951_87957953delinsTTT GRCh38
NC_000010.10:g.89717708_89717710delinsTTT , CM000672.1:g.89717708_89717710delinsTTT GRCh37
NC_000010.9:g.89707688_89707690delinsTTT NCBI36
NG_007466.2:g.99513_99515delinsTTT , LRG_311:g.99513_99515delinsTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.733_735delinsTTT ENSP00000514759.2:p.Gln245Phe
ENST00000710265.1:c.733_735delinsTTT ENSP00000518161.1:p.Gln245Phe
ENST00000472832.3:c.733_735delinsTTT ENSP00000483066.2:p.Gln245Phe
ENST00000688158.2:n.1468_1470delinsTTT
ENST00000688922.2:c.*563_*565delinsTTT ENSP00000508742.2:n.*563_*565delinsTTT
ENST00000700021.1:c.688_690delinsTTT ENSP00000514757.1:p.Gln230Phe
ENST00000700022.1:c.*72_*74delinsTTT ENSP00000514758.1:n.*72_*74delinsTTT
ENST00000700023.1:n.1891_1893delinsTTT
ENST00000700024.1:n.2125_2127delinsTTT
ENST00000700025.1:n.1502_1504delinsTTT
ENST00000700026.1:n.370_372delinsTTT
ENST00000700029.1:c.567_569delinsTTT
ENST00000706954.1:c.733_735delinsTTT ENSP00000516674.1:p.Gln245Phe
ENST00000706955.1:c.*768_*770delinsTTT ENSP00000516675.1:n.*768_*770delinsTTT
ENST00000686459.1:c.*319_*321delinsTTT ENSP00000508909.1:n.*319_*321delinsTTT
ENST00000688158.1:c.*844_*846delinsTTT ENSP00000509254.1:n.*844_*846delinsTTT
ENST00000688308.1:c.733_735delinsTTT ENSP00000508752.1:p.Gln245Phe
ENST00000688922.1:c.654_656delinsTTT
ENST00000693560.1:c.1252_1254delinsTTT ENSP00000509861.1:p.Gln418Phe
ENST00000371953.8:c.733_735delinsTTT MANE Select ENSP00000361021.3:p.Gln245Phe
ENST00000371953.7:c.733_735delinsTTT ENSP00000361021.3:p.Gln245Phe
ENST00000472832.2:c.160_162delinsTTT ENSP00000483066.1:p.Gln54Phe
NM_000314.5:c.733_735delinsTTT NP_000305.3:p.Gln245Phe
NM_000314.6:c.733_735delinsTTT NP_000305.3:p.Gln245Phe
NM_001304717.2:c.1252_1254delinsTTT NP_001291646.2:p.Gln418Phe
NM_001304718.1:c.142_144delinsTTT NP_001291647.1:p.Gln48Phe
XM_006717926.2:c.688_690delinsTTT XP_006717989.1:p.Gln230Phe
XM_011539981.1:c.733_735delinsTTT XP_011538283.1:p.Gln245Phe
XM_011539982.1:c.637_639delinsTTT XP_011538284.1:p.Gln213Phe
XR_945791.1:n.1303_1305delinsTTT
NM_000314.7:c.733_735delinsTTT NP_000305.3:p.Gln245Phe
NM_001304717.5:c.1252_1254delinsTTT NP_001291646.4:p.Gln418Phe
NM_001304718.2:c.142_144delinsTTT NP_001291647.1:p.Gln48Phe
NM_000314.8:c.733_735delinsTTT MANE Select NP_000305.3:p.Gln245Phe